Canonical Allele Identifier: PA1139726012
Gene: PRODH HGNC NCBI
ClinVar RCV:
RCV001053149
ClinVar Variation:
849233
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057419.5:p.Thr466Lys
CA410641923
NM_016335.6:c.1397C>A